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Dxn Pharmaceutical Sdn Bhd

FDA import alert and refusal historyJitra, MalaysiaFEI 3006649152

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Example subjectDxn Pharmaceutical Sdn Bh added to Import Alert 16-129 (red list)

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As of October 25, 2026, Dxn Pharmaceutical Sdn Bhd has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 6, 2026, was classified VAI (Voluntary Action Indicated).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Dxn Pharmaceutical Sdn Bhd

2 records, newest first. Each line links to the FDA page it came from.

2026

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2017

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Questions about Dxn Pharmaceutical Sdn Bhd

Is Dxn Pharmaceutical Sdn Bhd on an FDA import alert?
No listing for Dxn Pharmaceutical Sdn Bhd appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Malaysia page.
Has FDA refused shipments from Dxn Pharmaceutical Sdn Bhd?
No FDA import refusals for Dxn Pharmaceutical Sdn Bhd appear in FDA's refusal data since October 2016, as of October 25, 2026.
When was Dxn Pharmaceutical Sdn Bhd last inspected by FDA?
FDA's most recent inspection of Dxn Pharmaceutical Sdn Bhd with a final classification is dated March 6, 2026 and was classified VAI (Voluntary Action Indicated).
What is Dxn Pharmaceutical Sdn Bhd's FEI number?
Dxn Pharmaceutical Sdn Bhd's FDA Establishment Identifier (FEI) is 3006649152.

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Example subjectDxn Pharmaceutical Sdn Bh added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.